BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

354 related articles for article (PubMed ID: 20025873)

  • 21. Recombinant AAV-mediated gene delivery to the central nervous system.
    Tenenbaum L; Chtarto A; Lehtonen E; Velu T; Brotchi J; Levivier M
    J Gene Med; 2004 Feb; 6 Suppl 1():S212-22. PubMed ID: 14978764
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Influence of promoter and WHV post-transcriptional regulatory element on AAV-mediated transgene expression in the rat brain.
    Paterna JC; Moccetti T; Mura A; Feldon J; Büeler H
    Gene Ther; 2000 Aug; 7(15):1304-11. PubMed ID: 10918501
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Neonatal systemic delivery of scAAV9 in rodents and large animals results in gene transfer to RPE cells in the retina.
    Joussemet B; Belbellaa B; Mendes-Madeira A; Bucher T; Briot-Nivard D; Dubreil L; Colle MA; Cherel Y; Moullier P; Rolling F
    Exp Eye Res; 2011 Oct; 93(4):491-502. PubMed ID: 21723863
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Gene transfer into neurons from hippocampal slices: comparison of recombinant Semliki Forest Virus, adenovirus, adeno-associated virus, lentivirus, and measles virus.
    Ehrengruber MU; Hennou S; Büeler H; Naim HY; Déglon N; Lundstrom K
    Mol Cell Neurosci; 2001 May; 17(5):855-71. PubMed ID: 11358483
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Recombinant adeno-associated virus derived vectors (rAAV2) efficiently transduce ovarian and hepatocellular carcinoma cells--implications for cancer gene therapy.
    Małecki M; Swoboda P; Pachecka J
    Acta Pol Pharm; 2009; 66(1):93-9. PubMed ID: 19226976
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Differentiation of the RN33B cell line into forebrain projection neurons after transplantation into the neonatal rat brain.
    Lundberg C; Englund U; Trono D; Björklund A; Wictorin K
    Exp Neurol; 2002 Jun; 175(2):370-87. PubMed ID: 12061867
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Differential internalization and nuclear uncoating of self-complementary adeno-associated virus pseudotype vectors as determinants of cardiac cell transduction.
    Sipo I; Fechner H; Pinkert S; Suckau L; Wang X; Weger S; Poller W
    Gene Ther; 2007 Sep; 14(18):1319-29. PubMed ID: 17611587
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Gene marking of human neural stem/precursor cells using green fluorescent proteins.
    Navarro-Galve B; Villa A; Bueno C; Thompson L; Johansen J; Martínez-Serrano A
    J Gene Med; 2005 Jan; 7(1):18-29. PubMed ID: 15508144
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Gene delivery to the vasculature mediated by low-titre adeno-associated virus serotypes 1 and 5.
    Sen S; Conroy S; Hynes SO; McMahon J; O'Doherty A; Bartlett JS; Akhtar Y; Adegbola T; Connolly CE; Sultan S; Barry F; Katusic ZS; O'Brien T
    J Gene Med; 2008 Feb; 10(2):143-51. PubMed ID: 18067196
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina.
    Bainbridge JW; Mistry A; Schlichtenbrede FC; Smith A; Broderick C; De Alwis M; Georgiadis A; Taylor PM; Squires M; Sethi C; Charteris D; Thrasher AJ; Sargan D; Ali RR
    Gene Ther; 2003 Aug; 10(16):1336-44. PubMed ID: 12883530
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Local and retrograde gene transfer into primate neuronal pathways via adeno-associated virus serotype 8 and 9.
    Masamizu Y; Okada T; Kawasaki K; Ishibashi H; Yuasa S; Takeda S; Hasegawa I; Nakahara K
    Neuroscience; 2011 Oct; 193():249-58. PubMed ID: 21782903
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Tight regulation from a single tet-off rAAV vector as demonstrated by flow cytometry and quantitative, real-time PCR.
    Jiang L; Rampalli S; George D; Press C; Bremer EG; O'Gorman MR; Bohn MC
    Gene Ther; 2004 Jul; 11(13):1057-67. PubMed ID: 15152187
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Adeno-associated virus-mediated delivery of BCL-w gene improves outcome after transient focal cerebral ischemia.
    Sun Y; Jin K; Clark KR; Peel A; Mao XO; Chang Q; Simon RP; Greenberg DA
    Gene Ther; 2003 Jan; 10(2):115-22. PubMed ID: 12571640
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Efficient transduction of green fluorescent protein in spinal cord neurons using adeno-associated virus vectors containing cell type-specific promoters.
    Peel AL; Zolotukhin S; Schrimsher GW; Muzyczka N; Reier PJ
    Gene Ther; 1997 Jan; 4(1):16-24. PubMed ID: 9068791
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Lentiviral vector-mediated transduction of neural progenitor cells before implantation into injured spinal cord and brain to detect their migration, deliver neurotrophic factors and repair tissue.
    Blits B; Kitay BM; Farahvar A; Caperton CV; Dietrich WD; Bunge MB
    Restor Neurol Neurosci; 2005; 23(5-6):313-24. PubMed ID: 16477093
    [TBL] [Abstract][Full Text] [Related]  

  • 36. AAV2-mediated CLN2 gene transfer to rodent and non-human primate brain results in long-term TPP-I expression compatible with therapy for LINCL.
    Sondhi D; Peterson DA; Giannaris EL; Sanders CT; Mendez BS; De B; Rostkowski AB; Blanchard B; Bjugstad K; Sladek JR; Redmond DE; Leopold PL; Kaminsky SM; Hackett NR; Crystal RG
    Gene Ther; 2005 Nov; 12(22):1618-32. PubMed ID: 16052206
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Enhanced transduction of mouse bone marrow-derived dendritic cells by repetitive infection with self-complementary adeno-associated virus 6 combined with immunostimulatory ligands.
    Aldrich WA; Ren C; White AF; Zhou SZ; Kumar S; Jenkins CB; Shaw DR; Strong TV; Triozzi PL; Ponnazhagan S
    Gene Ther; 2006 Jan; 13(1):29-39. PubMed ID: 16136165
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Gene transfer to the spinal cord neural scar with lentiviral vectors: predominant transgene expression in astrocytes but not in meningeal cells.
    Hendriks WT; Eggers R; Verhaagen J; Boer GJ
    J Neurosci Res; 2007 Nov; 85(14):3041-52. PubMed ID: 17671987
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Recombinant AAV vectors containing the foot and mouth disease virus 2A sequence confer efficient bicistronic gene expression in cultured cells and rat substantia nigra neurons.
    Furler S; Paterna JC; Weibel M; Büeler H
    Gene Ther; 2001 Jun; 8(11):864-73. PubMed ID: 11423934
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sustained tetracycline-regulated transgene expression in vivo in rat retinal ganglion cells using a single type 2 adeno-associated viral vector.
    Folliot S; Briot D; Conrath H; Provost N; Cherel Y; Moullier P; Rolling F
    J Gene Med; 2003 Jun; 5(6):493-501. PubMed ID: 12797114
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.